Publicacións en colaboración con investigadores/as de Universidade de Santiago de Compostela (4)

2019

  1. Rare Variants in 48 Genes Account for 42% of Cases of Epilepsy With or Without Neurodevelopmental Delay in 246 Pediatric Patients

    Frontiers in Neuroscience, Vol. 13

2014

  1. A novel mutation in adamts13 of a child with upshaw-schulman syndrome

    Thrombosis and Haemostasis

2009

  1. Autosomal dominant C1149R von Willebrand disease: Phenotypic findings and their implications

    Haematologica, Vol. 94, Núm. 5, pp. 679-686

2002

  1. T-cell/histiocyte-rich large B-cell lymphoma is a disseminated aggressive neoplasm: Differential diagnosis from Hodgkin's lymphoma

    Histopathology, Vol. 41, Núm. 3, pp. 216-229